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Scope Warmer Base C3002

by Applied Medical Resources Corp.

Ref C3002Model Scope Warmer Bottle and Base

Scope Warmer Base C3002 is a device classified as Class I in the EU and Class II in the US made by Applied Medical Resources Corp., registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 0607915IR001LM) and listed in FDA GUDID since 13 Jul 2017 (UDI-DI 00607915116804), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0607915IR001LM Basic UDI-DI 00607915116804UDI-DIDate15 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00607915116804 UDI-DI Date13 Jul 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0607915IR001LM registered 15 Jul 2026 Active
  • FDA GUDID UDI-DI 00607915116804 listed 13 Jul 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00607915116804
  2. Registered EUDAMED 0607915IR001LM

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Applied Scope-Warmer System EUDAMED
Scope Warmer Base GUDID
Generic name
Instrument warmer, electric
Device name
Scope Warmer Bottle and Base
Model / reference
C3002, Scope Warmer Bottle and Base
Primary DI / UDI-DI
00607915116804
Basic UDI-DI
0607915IR001LM
Direct marketing DI
00607915116804
FDA product code
GCJ
EMDN code
Z12019099 Various instruments for general and multidisciplinary surgery - other
GMDN term
Instrument warmer, electric
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Instrument warmer, electric

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - OTHER.

Other devices from Applied Medical Resources Corp.

See all devices from Applied Medical Resources Corp. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)